Multiple Peroxisomal Enzymatic Deficiency Disorders: A Comparative Biochemical and Morphologic Study of Zellweger Cerebrohepatorenal Syndrome and Neonatal Adrenoleukodystrophy

Biologic, morphologic, and biochemical investigations performed in 2 patients demonstrate multiple peroxisomal deficiencies in the cerebrohepatorenal syndrome of Zellweger (CHRS) and neonatal adrenoleukodystrophy (NALD). Very long chain fatty acids, abnormal bile acids, including bile acid precursor...

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Hlavní autoři: Vamecq, Joseph, Draye, Jean-Pierre, Van Hoof, François, Misson, Jean-Paul, Evrard, Philippe, Verellen, Gaston, Eyssen, Hendrik J., Van Eldere, Johan, Schutgens, Ruud B. H., Wanders, Ronald J. A., Roels, Frank, Goldfischer, Sidney L.
Médium: Artigo
Jazyk:Inglês
Vydáno: 1986
Témata:
Rapid Communication
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1888479/
https://ncbi.nlm.nih.gov/pubmed/2879480
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